About: Bjarni V. Halldórsson

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About: Bjarni V. Halldórsson Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl)
rdfs:label	Bjarni V Halldórsson (es) Bjarni V. Halldórsson (de) Bjarni V. Halldórsson (en) Bjarni V. Halldórsson (nl) Bjarni V. Halldórsson (sl)
skos:prefLabel	Bjarni V Halldórsson (es) Bjarni V. Halldórsson (de) Bjarni V. Halldórsson (en) Bjarni V. Halldórsson (nl) Bjarni V. Halldórsson (sl)
name	Bjarni V Halldórsson (es) Bjarni V. Halldórsson (de) Bjarni V. Halldórsson (en) Bjarni V. Halldórsson (nl) Bjarni V. Halldórsson (sl)
Scopus author ID	wds:Q47502536-1EBB9B1C-7096-4872-B9FD-3CE249FE0D16
Scopus author ID	6603240812
given name	wds:Q47502536-076C6912-5265-4B4F-8B9D-F07574E4C7FE wds:Q47502536-f5eb663f-4209-069a-fbf3-61d6a2a11c82
given name	Bjarni Vilhjálmur
instance of	wds:Q47502536-69D911D6-7E38-454E-BC32-C6F0C2901681
instance of	Homo sapiens
zbMATH author ID	wds:Q47502536-2701432F-5A72-4375-9725-51FF5954ABB3
doctoral advisor	wds:Q47502536-5d216bed-459f-3a00-d833-2527450e3178
MR Author ID	wds:Q47502536-4dac6847-4126-6004-7feb-ae0d77090468
Mathematics Genealogy Project ID	wds:Q47502536-bda71095-4a92-eed2-f2d4-407bbb8b6ebb
zbMATH author ID	halldorsson.bjarni-v
doctoral advisor	Ramamurthy Ravi
MR Author ID	698404
Mathematics Genealogy Project ID	298085
skos:altLabel	Bjarni Halldórsson (en)
occupation	wds:Q47502536-E80B97B4-3393-4FB1-8676-6BBC44B4BD86
participant in	wds:Q47502536-0e817398-4811-7b19-9d00-bd90997476ae
sex or gender	wds:Q47502536-6643E977-06D6-44AB-B2F0-5B5766B8294F
DBLP author ID	wds:Q47502536-ECDFCEC4-D6A8-4214-9C4F-F46EE2FB38F8
date of birth	wds:Q47502536-2D78025F-0A20-443F-AACC-F86894119397
maintained by WikiProject	wds:Q47502536-06B9FCA5-C410-4AFD-B9CB-0983BE23F495
educated at	wds:Q47502536-b6ce2861-4fde-e6a8-10d3-be0ce30090ff
family name	wds:Q47502536-0700a9a4-4c82-4580-3e30-b4772360b803
DBLP author ID	https://dblp.org/pid/15/3605.rdf
occupation	researcher
participant in	International Mathematical Olympiad
sex or gender	male
DBLP author ID	15/3605
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
maintained by WikiProject	WikiProject Mathematics
educated at	Carnegie Mellon University
family name	Halldórsson
ORCID iD	wds:Q47502536-B572B80E-C830-4F36-A9AA-70CD5F1B7DDB
ORCID iD	https://orcid.org/0000-0003-0756-0767
ORCID iD	0000-0003-0756-0767
International Math...ad participant ID	wds:Q47502536-cc8d9988-4247-afbc-997c-26cc1002a96d
International Math...ad participant ID	3005
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q47502536
is author of	Many sequence variants affecting diversity of adult human height Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture Large-scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand Large recurrent microdeletions associated with schizophrenia Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22 A hybrid micro-macroevolutionary approach to gene tree reconstruction. Lessons from the past: familial aggregation analysis of fatal pandemic influenza (Spanish flu) in Iceland in 1918 Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. Impact of genetics on low bone mass in adults. New basal cell carcinoma susceptibility loci PopIns: population-scale detection of novel sequence insertions Comparative immunopeptidomics of humans and their pathogens Robustness of inference of haplotype block structure. Methylation of BoneSOST, Its mRNA, and Serum Sclerostin Levels Correlate Strongly With Fracture Risk in Postmenopausal Women KmerStream: streaming algorithms for k-mer abundance estimation. Genome-wide association study identifies 74 loci associated with educational attainment Optimal selection of SNP markers for disease association studies. The nature of nurture: Effects of parental genotypes. Identification of sequence variants influencing immunoglobulin levels. Multiple transmissions of de novo mutations in families DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis. Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits Graphtyper enables population-scale genotyping using pangenome graphs. A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis Characterizing mutagenic effects of recombination through a sequence-level genetic map Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis The nature of Neanderthal introgression revealed by 27,566 Icelandic genomes Islands of tractability for parsimony haplotyping. An integer programming formulation of the parsimonious loss of heterozygosity problem A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus.

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